Job Overview

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Compensation

Salary
Range $200,000.00 - $250,000.00
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Work Schedule

Standard Hours
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Benefits

Medical
Dental
Vision
health spending accounts
flexible spending accounts
Paid Time Off
Holidays
401k with match
paid family leave
Employee assistance program
short-term disability
long-term disability

Job Description

The American Red Cross is a humanitarian organization known worldwide for its dedication to helping people in need. Established over a century ago, it is the largest humanitarian network, providing relief to victims of disasters, supporting military families, and leading health and safety education programs. The American Red Cross operates with a mission to prevent and alleviate human suffering in the face of emergencies by mobilizing the power of volunteers and the generosity of donors. The organization is widely recognized for its blood donation programs, disaster relief efforts, and community resilience initiatives. With a robust network of volunteers and staff distributed across various regions, it combines compassion with professionalism to serve millions of people annually across the United States and beyond. Joining the American Red Cross means becoming part of a global force committed to making a difference and improving lives through service, innovation, and advocacy.

The position of Medical Director within the Therapeutic Apheresis and Cellular Therapeutics (TCS) programs at the American Red Cross is a crucial leadership role that plays an integral part in advancing the organization’s clinical services. This role involves providing expert clinical oversight and acting as a primary consultant for both internal teams and external healthcare partners. The Medical Director will be instrumental in shaping medical strategy and operations for regulated cellular therapies, including hematopoietic progenitor cells (HPCs), chimeric antigen receptor T-cell therapies (CAR-T), and Leukopaks. Responsibilities include policy development for cell collection, storage, and infusion, as well as partnering with executive leadership to expand collection footprints and optimize production of specialized cellular products.

This role emphasizes collaboration with various stakeholders to support program development, ensure compliance with regulatory standards such as FACT and FDA regulations, and elevate organizational clinical expertise. Additionally, the Medical Director will serve as the medical representative at institutional, regional, and national committees and act as a liaison for biotech partners. This position also entails regional responsibilities related to transfusion medicine, blood banking, and CLIA laboratory oversight, ensuring high standards of safety and quality in clinical and laboratory operations. The ideal candidate will have an MD or DO with board certification in Transfusion Medicine or Hematology/Oncology, extensive experience in cell therapy and stem cell transplantation, and a proven track record of leadership in medical program development. The position is remote with a requirement for regular onsite presence and travel, offering a competitive salary range of $200,000 to $250,000. This role presents a unique opportunity to contribute meaningfully to pioneering cellular therapies while joining a community committed to making a positive impact in healthcare and patient outcomes.

Job Requirements

  • MD/DO with board certification in Transfusion Medicine or Hematology/Oncology
  • Minimum of 5 years experience in Cell Therapy and Hematopoietic Stem Cell Transplantation preferred
  • Proven experience with FACT accreditation processes and AABB Standards
  • Knowledge of FDA regulations governing human cells tissues and cellular and tissue-based products
  • Prior leadership experience in program development
  • Ability to lead strategic growth and manage multidisciplinary teams
  • Compliance with FACT CLIA and FDA standards
  • Ability to travel regularly and maintain onsite presence as required
  • Combination of education and experience satisfying minimum requirements

Job Qualifications

  • MD/DO with board certification in Transfusion Medicine or Hematology/Oncology
  • Preference for a minimum of 5 years experience in Cell Therapy and Hematopoietic Stem Cell Transplantation but negotiable
  • Proven experience with FACT accreditation processes and AABB Standards for cellular therapy
  • Knowledge of FDA regulations governing human cells tissues and cellular and tissue-based products (HCT/Ps)
  • Demonstrate prior leadership experience in program development with knowledge of cellular therapy regulations transplant protocols and regulatory accreditation processes
  • Demonstrate ability to lead strategic growth manage multidisciplinary teams and maintain compliance with FACT CLIA and FDA standards
  • Experience leading or overseeing investigator-initiated clinical trials or translational research in cellular immunotherapy is of interest but not required

Job Duties

  • Direct medical strategy and operations for regulated cellular therapies including policy development for cell collection storage and infusion
  • Partner with executive leadership to expand collection footprints and optimize production of specialized cellular products like CAR-T starting materials
  • Contribute towards the expansion of cellular services through targeted outreach partnerships new program development and support of sales teams as required
  • Serve as the program’s medical office representative at institutional regional and national committees acting as the primary medical liaison for biotech partners providing expert guidance on donor eligibility product specifications and clinical trial alignment
  • Provide medical oversight for the transfer of client-specific protocols from research to clinical-grade production
  • Investigate and resolve donor recipient concerns transfusion issues and service complaints with timely leadership notification
  • Provide medical consultation in transfusion medicine blood banking and patient services to hospital clients fostering strong and collaborative relationships
  • Oversee medical aspects of regulated blood center operations including donor management recipient adverse reactions and product investigations
  • Provide oversight as CLIA laboratory director for a regional immunohematology reference laboratory as applicable
  • Contribute to the development of policies and procedures related to donor eligibility component quality and transfusion practices
  • Deliver continuing medical education to internal and external audiences promoting safe and effective use of blood components

Job Criteria

Experience

Mid Level (3-7 years)


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